25 results
·
29ms
·
Sources: EU EUDAMED, US FDA
HYPOALLERGENIC LATEX EXAMINATION GLOVES
FDA 510(k)
FDA Class 1
·General Hospital
LONG NAIL KIT R1.5, TI, LEFT GAMMA3 10X260MM X 12
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·September 6, 2012
ZAVATION
FDA UDI
Zavation LLC·00842166151598·WHITNEY 13mmx15mm , 0deg , 09mm
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756964906·LAP CHOLE PACK
Screw Removal Kit
FDA UDI
NOGA MEDICAL PRODUCTS LTD·07290118141228·Screw Removal Kit
Life Instruments
FDA UDI
Life Instrument Corporation·M93079100091R50·Frazier Suction Tube 9FR, OL of tube 15cm befor...
Kalitec Special
FDA UDI
Kalitec Direct LLC·B073DRK0100090·Dilator Sleeve, Screwdriver
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K1100090·Tray Insert 2, Cosmolock, Arcamed
Navagio
FDA UDI
Kalitec Direct LLC·B07330K1100090·Tray Insert
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1100090·Tray Insert
KOKO PEAK KP; KOKO PEAK KP+
FDA 510(k)
FDA Class 2
·Anesthesiology
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA 510(k)
FDA Class 2
·Cardiovascular
HUMERAL STEM 9MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·January 30, 2019
INSIGNIA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·January 11, 2013
MINI-CAP, DISCONNECT W/PVP-1SOLUTION
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·November 30, 2010
HEARTSTART ONSITE
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·February 24, 2014
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 26, 2024
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·July 15, 2020
ROADRUNNER UNIGLIDE HYDROPHILIC WIRE GUIDE
FDA Adverse Event
Malfunction
·COOK INC·Product code DQX·December 6, 2024
HUMERAL STEM 9MM
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code KWS·February 18, 2010